首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simple validated LC-MS/MS method for the determination of atropine and scopolamine in plasma for clinical and forensic toxicological purposes
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Simple validated LC-MS/MS method for the determination of atropine and scopolamine in plasma for clinical and forensic toxicological purposes

机译:经过简单验证的LC-MS / MS方法可测定血浆中的阿托品和东pol碱,用于临床和法医毒理学目的

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摘要

A liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the determination of atropine and scopolamine in 100 muL human plasma was developed and validated. Sample pretreatment consisted of protein precipitation with acetonitrile followed by a concentration step. Analytes and lev-obupivacaine (internal standard) were separated on a Zorbax XDB-CN column (75 mm x 4.6 mm i.d., 3.5 |xm) with gradient elution (purified water, acetonitrile, formic acid). The triple quadrupole MS was operated in ESI positive mode. Matrix effect was estimated for deproteinised plasma samples. Selected reaction monitoring (SRM) was used for quantification in the range of 0.10-50.00 ng/mL Interday precision for both tropanes and intraday precision for atropine was <10%, intraday precision for scopolamine was <14% and <18% at lower limit of quantification (LLOQ). Mean interday and intraday accuracies for atropine were within ±7% and for scopolamine within ±11%. The method can be used for determination of therapeutic and toxic levels of both compounds and has been successfully applied to a study of pharmacodynamic and pharmacokinetic properties of tropanes, where plasma samples of volunteers were collected at fixed time intervals after ingestion of a buckwheat meal, spiked with five low doses of tropanes.
机译:建立并验证了液相色谱-串联质谱法(LC-MS / MS)测定100μL人血浆中的阿托品和东pol碱的方法。样品预处理包括用乙腈沉淀蛋白质,然后进行浓缩步骤。在Zorbax XDB-CN色谱柱(75 mm x 4.6 mm i.d.,3.5μm)上用梯度洗脱(纯水,乙腈,甲酸)分离分析物和左旋布比卡因(内标)。三重四极杆质谱仪以ESI正模式运行。估计去蛋白血浆样品的基质效应。使用选定的反应监测(SRM)在0.10-50.00 ng / mL范围内进行定量测定,对环烷的日内精密度和阿托品的日内精密度<10%,东pol碱的日内精密度<14%,下限<18%量化(LLOQ)。阿托品的平均日间和日内准确度在±7%之内,东pol碱的平均日内准确性在±11%之内。该方法可用于测定这两种化合物的治疗和毒性水平,并已成功地用于研究托烷的药效学和药代动力学特性,其中在摄入荞麦粉后以固定的时间间隔收集志愿者的血浆样品,加标五种低剂量的托烷。

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